Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41612318A>G | CA217380 | KRT16 | c.371T>C (p.Leu124Pro) n.448T>C c.-312-32T>C (n.-312-32T>C) | ClinVar dbSNP |
17 | g.41612318A>C | CA217381 | KRT16 | c.371T>G (p.Leu124Arg) n.448T>G c.-312-32T>G (n.-312-32T>G) | ClinVar dbSNP |
17 | g.41612318A>T | CA217379 | KRT16 | c.371T>A (p.Leu124His) n.448T>A c.-312-32T>A (n.-312-32T>A) | ClinVar dbSNP |